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FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

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1. scibot 03 Apr 2026
  
  in Public
  
  BL 60756
  
  DOI: 10.64898/2026.03.27.26349271
  
  Resource: RRID:BDSC_60756
  
  Curator: @scibot
  
  SciCrunch record: RRID:BDSC_60756
  
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  RRID:BDSC_60756
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RRID:BDSC_60756

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scibot

URL

medrxiv.org/content/10.64898/2026.03.27.26349271v1
Mar 2023
www.sciencedirect.com www.sciencedirect.com

Neuronal identity defines α-synuclein and tau toxicity

1
1. scibot 28 Mar 2023
  
  in Public
  
  RRID:BDSC_60756
  
  DOI: 10.1016/j.neuron.2023.02.033
  
  Resource: RRID:BDSC_60756
  
  Curator: @scibot
  
  SciCrunch record: RRID:BDSC_60756
  
  What is this?
  
  RRID:BDSC_60756
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RRID:BDSC_60756

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scibot

URL

sciencedirect.com/science/article/pii/S0896627323001666